Attention: This repository is under review for potential modification in compliance with Administration directives.

Important Notice:
NICHD is in the process of migrating DASH to a new platform. DASH is providing support for new study submissions during the migration. Email DASHCurator@mail.nih.gov with study submission inquiries.

Please contact SupportDASH@mail.nih.gov with all other inquiries. We appreciate your patience during this transition.

Document Detail

De-identification Method

Type: De-Identification Methodology Study: Molecular Bases of Response to Copper Treatment in Menkes Disease, Related Phenotypes, and Unexplained Copper Deficiency

Document Information

Document Type: De-Identification Methodology

Study: Molecular Bases of Response to Copper Treatment in Menkes Disease, Related Phenotypes, and Unexplained Copper Deficiency

Description:

De-identification Method

Study Information

Study Abbreviation: 09-CH-0059

Clinical Research Network: Other Initiatives

Data Collection Start: 2009-02-27

Data Collection End: 2019-11-27

Study Population: 93

Study Demographics

Subjects by Sex

Males
Females

Subjects by Ethnicity

Hispanic
Non-Hispanic
Unknown

Subjects by Race

American Indian or Alaska Native
Asian
Black or African American
White
Multi Race
Unknown

Subjects by Life Stage

Infant (0 - 1 yr)
Toddler (13 mo - <2 yrs)
Early Childhood (2 - 5 yrs)
Middle Childhood (6 - 11 yrs)
Adults
Unknown

Aggregate Demographics

Male: 88

Female: 5

White: 60

Black: 8

Hispanic: 12

Non-Hispanic: 79

NIH...Turning Discovery Into Health ®